×
Register Here to Apply for Jobs or Post Jobs. X
More jobs:

Quality Project Lead- FTC

Job in Midrand, Gauteng, South Africa
Listing for: Biopharma Careers
Full Time, Contract position
Listed on 2026-09-13
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
    Data Scientist
Job Description & How to Apply Below

Project lead for Analytical Method transfers and post-importation testing exemption application management

Major Accountabilities:

  • Establish and maintain a prioritised tracker for all post importation exemption applications. Coordinate supporting documents from manufacturing sites and relevant functions. Compile and quality-check submission packages. Coordinate submission applications, proof of payment and respond to Health Authority queries. Escalate overdue inputs through established governance channels.
  • Analytical Method transfer:
    1) Lead end-to-end method transfer schedules between sites and the local laboratory,
    2) Draft, review, and approve method transfer plans, protocols, comparative testing strategies, acceptance criteria, and final reports.
    3) Act as the Subject Matter Expert (SME) to resolve out-of-specification (OOS) results, deviations, and analytical challenges,
    4) Ensure equipment and reference standards are available
  • Complete an orderly handover at the end of the project.
Key Performance Indicators:
  • Adherence to cGMP and SOPs
  • Project targets are met
  • Quality related processes carried out in a timely way
  • GxP risks proactively identified and effectively mitigated
  • Timely close out of deviations, out of specifications and corrective and preventative actions
  • Compliance with all aspects of the Code of Conduct/ Novartis Policies and Procedures
Minimum Requirements:
  • Work Experience:
  • Managed health authority submissions and applied guidelines to ensure compliance.
  • Engaged with SAHPRA on regulatory, quality, and compliance-related matters.
  • Post-importation testing exemption and analytical method transfer.
  • Collaborated with Quality Control (QC) laboratories to support testing, investigations, and compliance requirements.
Skills:
  • Knowledge and understanding of GMP, quality systems and quality and regulatory practices
  • Understanding and interpretation of regulations & guidelines
  • Document management
  • Analytical thinking and problem solving

    Project management
  • Planning & organizing
  • Good time management
  • High compliance
  • Communication and interpersonal skills.
  • Self Awareness
Languages :
  • English.
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary